Investigating ultrastructural morphology in MIRAGE syndrome-derived fibroblasts using transmission electron microscopy. [version 2; peer review: 1 approved, 2 approved with reservations]
Background Heterozygous de novo variants in the gene SAMD9 cause the complex multisystem disorder, MIRAGE syndrome. Patients are characterised by myelodysplasia, infections, growth restriction, adrenal insufficiency, gonadal dysfunction and enteropathies. Pathogenic variants in SAMD9 are gain-of-fun...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
F1000 Research Ltd
2024-02-01
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Series: | F1000Research |
Subjects: | |
Online Access: | https://f1000research.com/articles/12-155/v2 |